New Delhi [India], March 5 (ANI): Observing rare disease Awareness day on 28th February 2019, Dr. Lal PathLabs Ltd. has associated with Organization of Rare Disease India (ORDI) for a campaign “Rare Needs Care”. A leading diagnostic and related healthcare service provider, Dr. Lal PathLabs L
New Delhi [India], Dec 18 (ANI): The Central government has filed an affidavit in the Delhi High Court, underlying need to re-frame the policy for rare diseases which was finalised and approved last year.
New Delhi [India] October 15 (ANI): A Public Interest Litigation (PIL) has been filed in the Supreme Court against the Centre and state governments for "failing to constitute a state-level technical-cum-administrative committee, and to identify designated hospitals for treatment of people s
New Delhi [India], May 26 (ANI): The Ministry of Health & Family Welfare (MoH&FW), in 2017, took a landmark step by approving the National Policy for Treatment of Rare Diseases.
New Delhi [India], Apr 21 (ANI): Organisation for Rare Disease India (ORDI), a non-profit patient association focusing on improving the health of patients with rare diseases, has taken the initiative to appeal to the state governments to implement individual state rare disease policies as pe
New Delhi [India], Mar 08 (ANI): Rare diseases, which are often referred to as orphan diseases, are estimated to have impacted 72-96 million people in India. The Indian government has now put a National Rare Disease Policy in place and Rs 100 crore funds have been allocated towards genetic d
New Delhi [India], Feb 9 (ANI): As an important step towards expediting the process of providing treatment to rare disease patients, the Delhi state government, in the High Court, has proposed the setting up of a Technical cum Administrative Committee for rare diseases.
Washington D.C. [USA], Dec 20 (ANI): People living with rare diseases are at greater risk of experiencing poor quality of life such as increased levels of anxiety, depression, pain, fatigue.
New Delhi [India], Nov 24 (ANI): Putting the focus on rare diseases, experts have laid emphasis on ensuring timely treatment for the patients. Although very few people are affected by these disorders, rare diseases are often chronic and severe and make the life of a patient debilitating.
Chennai (Tamil Nadu) [India], Oct 17 (ANI): Emphasising on the importance of timely treatment for Lysosomal Storage Disorders (LSDs), medical experts urged for concrete steps to be taken in this direction.